dentin dysplasia

Preferred Label : dentin dysplasia;

MeSH definition : An apparently hereditary disorder of dentin formation, marked by a normal appearance of coronal dentin associated with pulpal obliteration, faulty root formation, and a tendency for peripheral lesions without obvious cause. (From Dorland, 27th ed);

MeSH synonym : dentin dysplasias; dysplasia, dentin; dysplasias, dentin;

MeSH annotation : a tooth abnorm; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES;

Wikipedia link : https://en.wikipedia.org/wiki/Dentin dysplasia;

Details

Origin ID

D003805;

UMLS CUI

C0011430;

Allowable qualifiers
- blood [MeSH Qualifier]
- cerebrospinal fluid [MeSH Qualifier]
- chemically induced [MeSH Qualifier]
- classification [MeSH Qualifier]
- complications [MeSH Qualifier]
- diagnosis [MeSH Qualifier]
- diagnostic imaging [MeSH Qualifier]
- diet therapy [MeSH Qualifier]
- drug therapy [MeSH Qualifier]
- economics [MeSH Qualifier]
- embryology [MeSH Qualifier]
- enzymology [MeSH Qualifier]
- epidemiology [MeSH Qualifier]
- ethnology [MeSH Qualifier]
- etiology [MeSH Qualifier]
- genetics [MeSH Qualifier]
- history [MeSH Qualifier]
- immunology [MeSH Qualifier]
- metabolism [MeSH Qualifier]
- microbiology [MeSH Qualifier]
- mortality [MeSH Qualifier]
- nursing [MeSH Qualifier]
- parasitology [MeSH Qualifier]
- pathology [MeSH Qualifier]
- physiopathology [MeSH Qualifier]
- prevention and control [MeSH Qualifier]
- psychology [MeSH Qualifier]
- radiotherapy [MeSH Qualifier]
- rehabilitation [MeSH Qualifier]
- surgery [MeSH Qualifier]
- therapy [MeSH Qualifier]
- urine [MeSH Qualifier]
- veterinary [MeSH Qualifier]
- virology [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- Dentine dysplasia [ICD-11 Subcategory]
- Dentinogenesis imperfecta limited to primary teeth [HPO term]
- Hereditary disturbances in tooth structure, not elsewhere classified [ICD-10 Sub-category]
- Hereditary disturbances in tooth structure, not elsewhere classified [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Dentin dysplasia [ORDO Disease]
- Dentin dysplasia (disorder) [SNOMED CT concept]
- dentin dysplasia [DO Concept]
- dentin dysplasia [Disease (Nov.)]
DO Cross reference
- dentin dysplasia [DO Concept]
HPO term
- Dentinogenesis imperfecta limited to primary teeth [HPO term]
Manual BTNT mappings - CISMeF
- Dentin dysplasia type I [ORDO Disease]
- Dentin dysplasia-sclerotic bones syndrome [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Hereditary dentin defect [ORDO Disease]
ORDO relation(s)
- Dentin dysplasia [ORDO Disease]
Record concept(s)
- dentin dysplasia [MeSH concept]
Related MeSH Supplementary Concept(s)
- dentin dysplasia sclerotic bones [MeSH Supplementary Concept]
- dentin dysplasia, type 1 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dentin dysplasia [ORDO Disease]
- Dentin dysplasia [HPO term]
- Dentin dysplasia (disorder) [SNOMED CT concept]
- dentin dysplasia [DO Concept]
- dentin dysplasia [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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